TENZCARE DUAL-CHANNEL STIMULATOR
K-Number: K800758 · 1980-04-10
Advertisement
Device Summary
Frequently Asked Questions
What is the TENZCARE DUAL-CHANNEL STIMULATOR?
TENZCARE DUAL-CHANNEL STIMULATOR is a medical device that received FDA 510(k) clearance on 1980-04-10. The listed applicant is 3M Company. The 510(k) number is K800758.
When did TENZCARE DUAL-CHANNEL STIMULATOR receive FDA 510(k) clearance?
TENZCARE DUAL-CHANNEL STIMULATOR received FDA 510(k) clearance on 1980-04-10, under 510(k) number K800758.
Who is the listed applicant for TENZCARE DUAL-CHANNEL STIMULATOR?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENZCARE DUAL-CHANNEL STIMULATOR?
The FDA product code for TENZCARE DUAL-CHANNEL STIMULATOR is GZJ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing 3M Company as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GZJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement